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A multicomponent tetrazolo indole synthesis
The ubiquitous presence of the indole fragment in natural products and drugs asks for ever novel syntheses. We report an unprecedented mild, two-step synthesis of 2-tetrazolo substituted indoles based on the Ugi-tetrazole reaction combined with an acidic ring closure. A gram-scale synthesis, a bioac...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259579/ https://www.ncbi.nlm.nih.gov/pubmed/34128009 http://dx.doi.org/10.1039/d1cc02384e |
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author | Lei, Xiaofang Lampiri, Panagiota Patil, Pravin Angeli, Giasemi Neochoritis, Constantinos G. Dömling, Alexander |
author_facet | Lei, Xiaofang Lampiri, Panagiota Patil, Pravin Angeli, Giasemi Neochoritis, Constantinos G. Dömling, Alexander |
author_sort | Lei, Xiaofang |
collection | PubMed |
description | The ubiquitous presence of the indole fragment in natural products and drugs asks for ever novel syntheses. We report an unprecedented mild, two-step synthesis of 2-tetrazolo substituted indoles based on the Ugi-tetrazole reaction combined with an acidic ring closure. A gram-scale synthesis, a bioactive compound and further transformations were performed. |
format | Online Article Text |
id | pubmed-8259579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-82595792021-07-16 A multicomponent tetrazolo indole synthesis Lei, Xiaofang Lampiri, Panagiota Patil, Pravin Angeli, Giasemi Neochoritis, Constantinos G. Dömling, Alexander Chem Commun (Camb) Chemistry The ubiquitous presence of the indole fragment in natural products and drugs asks for ever novel syntheses. We report an unprecedented mild, two-step synthesis of 2-tetrazolo substituted indoles based on the Ugi-tetrazole reaction combined with an acidic ring closure. A gram-scale synthesis, a bioactive compound and further transformations were performed. The Royal Society of Chemistry 2021-06-09 /pmc/articles/PMC8259579/ /pubmed/34128009 http://dx.doi.org/10.1039/d1cc02384e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Lei, Xiaofang Lampiri, Panagiota Patil, Pravin Angeli, Giasemi Neochoritis, Constantinos G. Dömling, Alexander A multicomponent tetrazolo indole synthesis |
title | A multicomponent tetrazolo indole synthesis |
title_full | A multicomponent tetrazolo indole synthesis |
title_fullStr | A multicomponent tetrazolo indole synthesis |
title_full_unstemmed | A multicomponent tetrazolo indole synthesis |
title_short | A multicomponent tetrazolo indole synthesis |
title_sort | multicomponent tetrazolo indole synthesis |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259579/ https://www.ncbi.nlm.nih.gov/pubmed/34128009 http://dx.doi.org/10.1039/d1cc02384e |
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